Phase IV trials are conducted “in the real world.” As such, they can complement, and in certain circumstances, replace Phase III trials. But we can get you the patients you need quickly. Read the details of what happens in a clinical research study, from screening to arriving on the first day to your last study visit. However, where more thorough investigation is required, a Phase IIIb clinical trial or a Phase IV trial may be required. We deliver a patient-centric ecosystem of conveniently located resources all connected by a single technology platform. COVANCE is a registered trademark and the marketing name for Covance Inc. and its subsidiaries around the world.What are Decentralized Clinical Trials, Virtual Clinical and Hybrid Clinical Trials?When should Phase IV trials be considered for drug development?How can Phase IV studies/trials, and Phase IIIb trials be combined to explore new indications?How does Covance utilize proprietary data to improve clinical study outcomes?What is the Covance Integrated Clinical Pharmacology Solution?How the RACE for Children Act Impacts Pediatric Oncology Drug DevelopmentView this webinar to get insights spanning rare diseases, regulatory strategy, oncology and pediatric drug development. Through new approaches explored, ideas perfected, and transformational thinking.Covance, the drug development business of LabCorp, is recognized as a leader in drug development because of our exceptional people. We’ll help find the clinical trial that’s right for you. Some studies require both overnight stays and outpatient visits (OPVs).Read all the Frequently Asked Questions about payment. Men and women can be affected differently by medications. But we can get you the patients you need quickly. Contract Research Organization (CRO) and Clinical Trials Covance, a global contract research organization and drug development services company, has … Check out all the options that we currently offer. Travel restrictions, social distancing and the fear of contracting the disease are impeding conventional trial conduct. M-F: 10:00 AM - 3:00 PM EST (9:00 AM - 2:00 PM CST). Learn how to accelerate patient recruitment and optimize protocol design while reducing patient burden and increasing retention. M-F: 10:00 AM - 3:00 PM EST (9:00 AM - 2:00 PM CST). A development process that usually spans several years is being compressed into one year - or less. Better. And it’s our mission to help speed that process. An integrated development platform, including the resources, experience, expertise and infrastructure necessary to design and execute early clinical studies is an effective way of mitigating risk. An increasing number of pharmaceutical and biotech companies are turning toward this model to decrease their overhead and make their operations leaner and more efficient. And Faster. What matters is not “how it’s always been done,” but how it can be done now. COVANCE is a registered trademark and the marketing name for Covance Inc. and its subsidiaries around the world.Reach IND/CTA quickly with a programmatic approach or choose from thousands of studies.Remove roadblocks to early & late trials with intelligent recruitment, integrated project delivery and therapeutic expertise.Maximize your product’s value and ensure patients have access to safe and effective treatments.Comprehensive laboratory support for all phases of clinical trials.Meet global crop protection and chemical guidelines with expertise paired with regulatory insights.Leverage a specialized team and powerful collection of resources for every step of product development.Improve clinical study outcomes with unrivaled, proprietary data and technology.COVID-19: vaccine innovation and safety at pandemic speedThe global spread of COVID-19 and its great impact on the health and wellbeing of our population has imposed a race to develop an effective vaccine at unprecedented speed. Getting patients for clinical lung disease or disorder trials like asthma, COPD, cystic fibrosis, lower respiratory infections, or idiopathic pulmonary fibrosis (IPF), interstitial lung disease, and acute respiratory distress syndrome isn't easy. Facing ever … See where you’ll spend time in our clinical trial facilities and what to expect during the study. An example of a DCT model is our solution that includes connecting LabCorp’s U.S.-based Patient Service Centers, global partnerships with reputable retail pharmacies, as well as home health phlebotomy and nursing service providers, with a best-in-class technology platform. Let’s discuss your options and find out if you qualify for a paid clinical research study. Check out all the options that we currently offer. LabCorp has announced that Covance has completed the transaction to acquire GlobalCare, a globally recognized industry leader in patient-centric decentralized clinical trials (DCTs). Covance FSPx® is the functional service provider you can rely on to deliver customizable solutions through strong collaboration and commitment to quality. Every day, thousands of people like you participate in clinical research studies. The need to transition from a site-centric approach to a more patient-centric clinical trial model led to innovations that reduce patient burden by reducing the amount of travel needed, allowing more services to be performed at or near the patients’ homes and incorporate new ways of identifying and enrolling trial participants. This approach blends a global patient support ecosystem with technology to allow patients to participate in clinical research from virtually anywhere.Whether you are developing a COVID-19 assay, a vaccine to prevent patients from getting COVID-19, an antiviral or a treatment to mitigate the severe immunological response (cytokine storm) associated with COVID-19, we can partner with you to provide critical drug development and diagnostic services to address the global pandemic.The healthcare industry is always looking to the future... to discover a better treatment... to deliver a cure... to prevent disease…to improve quality of life.

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